CLASS II Drug recall · Reported 3 Jun 2015 · FDA Enforcement Report
Sodium Hyaluronate Prefilled Syringe) Sterile Water 20MG/ML recalled
Advanced Physician Solutions is recalling Sodium Hyaluronate Prefilled Syringe) Sterile Water 20MG/ML Injectable, Advanced, distributed nationwide in the US. The recall was initiated on 18 May 2015 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-1103-2015
- FDA event ID
- 71205
- Recalling firm
- Advanced Physician Solutions, N Hollywood, CA
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 18 May 2015
- FDA classified
- 28 May 2015
- Reported
- 3 Jun 2015
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Foreign Material
- Drug class
- Injectable & IV Drugs
Timeline
| 18 May 2015 | Recall initiated by company | |
| 28 May 2015 | Classified by FDA | +10 days |
| 3 Jun 2015 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Lack of Assurance of Sterility
Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.
Product as listed by the FDA
SODIUM HYALURONATE (2ML PREFILLED SYRINGE) STERILE WATER 20MG/ML INJECTABLE, Advanced Compounding Pharmacy, 7225 Fulton Ave., North Hollywood, CA 91605
Where it was distributed
Nationwide
Questions about this recall
Is Sodium Hyaluronate Prefilled Syringe) Sterile Water 20MG/ML Injectable, Advanced recalled?
Yes. Advanced Physician Solutions recalled Sodium Hyaluronate Prefilled Syringe) Sterile Water 20MG/ML Injectable, Advanced on 18 May 2015. The recall is Class II and its status is Terminated. Recall number D-1103-2015.
Why was it recalled?
Lack of Assurance of Sterility
Which lots are affected?
All lots
Where was it sold?
Nationwide
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Advanced Physician Solutions
All 18| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Glycerin (Sterile Water) 71% Injectable recalled | Advanced Physician Solutions | Foreign Material | Nationwide |
| Drug | CLASS II | Estradiol Cypionate (Sesame Oil) Vial 5MG/ML Injectable recalled | Advanced Physician Solutions | Foreign Material | Nationwide |
| Drug | CLASS II | Cyanocobalamin (Paraben Water) Vial) 2000MCG/ML Injectable recalled | Advanced Physician Solutions | Foreign Material | Nationwide |
| Drug | CLASS II | Sodium Tetradecyl (Sterile Water) Vial 2% Injectable recalled | Advanced Physician Solutions | Foreign Material | Nationwide |
| Drug | CLASS II | Vitamin D3 (Olive Oil) Vial)/ML Injectable recalled | Advanced Physician Solutions | Foreign Material | Nationwide |